Clinical data | |
---|---|
AHFS/ Drugs.com | International Drug Names |
Routes of administration | Oral |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
Chemical and physical data | |
Formula | C20H27NO4 |
Molar mass | 345.439 g·mol−1 |
3D model ( JSmol) | |
Chirality | Racemic mixture |
| |
| |
(verify) |
Bevantolol ( INN) was a drug candidate for angina and hypertension that acted as both a beta blocker and a calcium channel blocker. [1] [2] It was discovered and developed by Warner-Lambert [3] but in January 1989 the company announced that it had withdrawn the New Drug Application; the company's chairman said: "Who needs the 30th beta blocker?" [4] As of 2016 [update] it wasn't marketed in the US, UK, or Europe and the authors of a Cochrane review could find no product monograph for it. [5]
Clinical data | |
---|---|
AHFS/ Drugs.com | International Drug Names |
Routes of administration | Oral |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
Chemical and physical data | |
Formula | C20H27NO4 |
Molar mass | 345.439 g·mol−1 |
3D model ( JSmol) | |
Chirality | Racemic mixture |
| |
| |
(verify) |
Bevantolol ( INN) was a drug candidate for angina and hypertension that acted as both a beta blocker and a calcium channel blocker. [1] [2] It was discovered and developed by Warner-Lambert [3] but in January 1989 the company announced that it had withdrawn the New Drug Application; the company's chairman said: "Who needs the 30th beta blocker?" [4] As of 2016 [update] it wasn't marketed in the US, UK, or Europe and the authors of a Cochrane review could find no product monograph for it. [5]